2-(trimethylsilyl)ethyl 2-bromo-7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-5H-thiazolo[3,2-a]-pyridine-3-carboxylate

Base Information

Chemical Name:2-(trimethylsilyl)ethyl 2-bromo-7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-5H-thiazolo[3,2-a]-pyridine-3-carboxylate
CAS No.:1345974-40-4
Molecular Formula:C₃₁H₂₇BrF₃NO₃SSi
Molecular Weight:658.611
Hs Code.:

Synonyms:2-(trimethylsilyl)ethyl 2-bromo-7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-5H-thiazolo[3,2-a]-pyridine-3-carboxylate

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Chemical Property of 2-(trimethylsilyl)ethyl 2-bromo-7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-5H-thiazolo[3,2-a]-pyridine-3-carboxylate

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Technology Process of 2-(trimethylsilyl)ethyl 2-bromo-7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-5H-thiazolo[3,2-a]-pyridine-3-carboxylate

There total 5 articles about 2-(trimethylsilyl)ethyl 2-bromo-7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-5H-thiazolo[3,2-a]-pyridine-3-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 83.0%

: 1345974-38-0
(3RS)-2-(trimethylsilyl)ethyl 7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-3,5-dihydro-2H-thiazolo-[3,2-a]pyridine-3-carboxylate

: 1345974-40-4
2-(trimethylsilyl)ethyl 2-bromo-7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-5H-thiazolo[3,2-a]-pyridine-3-carboxylate

Guidance literature:: With Bromotrichloromethane; sodium hydride; In 2-(Trimethylsilyl)ethanol; acetonitrile; at 20 ℃; for 10h;
DOI:10.1021/jo201952p

Reference yield:

: 7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid

: 1345974-40-4
2-(trimethylsilyl)ethyl 2-bromo-7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-5H-thiazolo[3,2-a]-pyridine-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.17 h / 20 °C

2: dichloromethane / 0.25 h / 20 °C

3: Bromotrichloromethane; sodium hydride / 2-(Trimethylsilyl)ethanol; acetonitrile / 10 h / 20 °C

With oxalyl dichloride; Bromotrichloromethane; sodium hydride; N,N-dimethyl-formamide; In dichloromethane; 2-(Trimethylsilyl)ethanol; acetonitrile;
DOI:10.1021/jo201952p

Reference yield:

: 864365-23-1
(3R)-7-naphthalen-1-ylmethyl-5-oxo-8-(3-(trifluoromethyl)phenyl)-2,3-dihydro-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

: 1345974-40-4
2-(trimethylsilyl)ethyl 2-bromo-7-(naphthalen-1-ylmethyl)-5-oxo-8-(3-(trifluoromethyl)phenyl)-5H-thiazolo[3,2-a]-pyridine-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: lithium hydroxide / tetrahydrofuran / 0.25 h / 20 °C

2: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.17 h / 20 °C

3: dichloromethane / 0.25 h / 20 °C

4: Bromotrichloromethane; sodium hydride / 2-(Trimethylsilyl)ethanol; acetonitrile / 10 h / 20 °C

With oxalyl dichloride; Bromotrichloromethane; sodium hydride; N,N-dimethyl-formamide; lithium hydroxide; In tetrahydrofuran; dichloromethane; 2-(Trimethylsilyl)ethanol; acetonitrile;
DOI:10.1021/jo201952p